1248826-72-3 Usage
Uses
Used in Organic Synthesis:
2,3-Pyrrolidinedione, 4,4-diMethylis used as a protecting group for amines in organic synthesis for the following reasons:
Its stability under a variety of conditions allows for versatile applications in the synthesis of various organic compounds.
As a protecting group, it helps prevent unwanted reactions with the amine group during the synthesis process, ensuring the desired product is obtained.
Used in Pharmaceutical Industry:
2,3-Pyrrolidinedione, 4,4-diMethylis used as an intermediate in the synthesis of certain pharmaceutical compounds for the following reasons:
Its unique chemical structure and properties make it a valuable building block in the development of new drugs.
Its use in protecting amines can be crucial in the synthesis of complex molecules with specific biological activities.
Used in Chemical Research:
2,3-Pyrrolidinedione, 4,4-diMethylis used as a research tool in chemical studies for the following reasons:
Its reactivity and stability make it an interesting subject for understanding the behavior of pyrrolidine-based compounds.
It can be used to explore new reaction pathways and mechanisms in organic chemistry, potentially leading to the discovery of novel synthetic methods or compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1248826-72-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,8,8,2 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1248826-72:
(9*1)+(8*2)+(7*4)+(6*8)+(5*8)+(4*2)+(3*6)+(2*7)+(1*2)=183
183 % 10 = 3
So 1248826-72-3 is a valid CAS Registry Number.
1248826-72-3Relevant academic research and scientific papers
Straightforward preparation of enantiopure 3-amino-4,4-dimethylpyrrolidin- 2-one and its derivatives
Camps, Pelayo,Munoz-Torrero, Diego,Rull, Jordi,Mayoral, Jose Antonio,Calvet, Teresa,Font-Bardia, Merc
experimental part, p. 2124 - 2135 (2010/10/03)
An easy access to both enantiomers of 3-amino- and 3-(dimethylamino)-4,4- dimethylpyrrolidin-2-one from rac-pantolactam using (R)-α- methylbenzylamine as a chiral auxiliary is described.
